Needle assembly

ABSTRACT

A blood collection set including a non-patient needle assembly interconnected with an intravenous needle assembly through tubing is provided. The non-patient needle assembly includes a hub assembly adapted for mounting with a blood collection set, and an internal blunting member including a blunted tip. The non-patient needle assembly further includes an external cannula concentric with the internal blunting member and including a non-patient puncture tip adjacent the blunted tip. The external cannula is axially displaceable with respect to the hub assembly between a first retracted position in which the non-patient puncture tip extends beyond the blunted tip and a second activated position in which blunted tip extends beyond the non-patient puncture tip.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No.11/170,130 filed Jun. 29, 2005, now U.S. Pat. No. 7,678,076, which is adivisional application of U.S. patent application Ser. No. 10/173,928filed Jun. 17, 2002, (now abandoned), which claims priority to U.S.Provisional Patent Application No. 60/377,399 filed May 2, 2002, theentire disclosures of each of which are hereby incorporated byreference.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to needle assemblies having a bluntingelement for safe and convenient handling. More particularly, the presentinvention relates to a non-patient needle assembly which includes ablunting element for the non-patient needle for use in connection with ablood collection set.

2. Description of Related Art

Disposable medical devices having piercing elements are typically usedfor administering a medication or withdrawing a fluid, such as bloodcollecting needles, fluid handling needles, and assemblies thereof.Current medical practice requires that the fluid containers and needleassemblies used in such systems be inexpensive and readily disposable.Consequently, existing blood collection systems, for example, typicallyemploy some form of durable, reusable holder on which detachable anddisposable needles and fluid collection tubes may be mounted. A bloodcollection system of this nature can be assembled prior to use and thendisassembled after usage. Thus, these blood collection systems allowrepeated use of the relatively expensive holder upon replacement of therelatively inexpensive needle and/or fluid collection tube. In additionto reducing the cost of collecting blood specimens, these bloodcollection systems also help minimize the production of hazardousmedical waste.

Conventional intravenous tubing sets are commonly employed for use inconnection with blood collection. A particularly useful intravenoustubing set for such application is the VACUTAINER® Brand Safety-Lok™Blood Collection Set, available from Becton, Dickinson and Company ofFranklin Lakes, N.J. Such a blood collection set includes an intravenousneedle assembly attached to one end of a tube, with the other end of thetube connected to a blood collection needle assembly including a stopperpuncture needle, or a “non-patient” puncture needle. In use, theintravenous needle assembly is inserted into the vein of a patient, anda tube holder is attached to the blood collection needle assembly. Anevacuated tube is inserted into the tube holder, and the stopperpuncture needle or non-patient puncture needle punctures the stopper ofthe tube, allowing blood to flow into the tube.

In order to reduce the risk of incurring an accidental needle-stickwound, protection of used needle tips becomes important. With concernabout infection and transmission of diseases, methods and devices toenclose the used disposable needle have become very important and ingreat demand. Many arrangements have been designed for protecting usedneedle tips. For example, U.S. Pat. No. 5,120,320 to Fayngold and U.S.Pat. No. 5,192,275 to Burns disclose safety shields for use inconnection with the intravenous needle assembly of such blood collectionassemblies. The safety shield covers and protects the intravenous needleassembly after use. Also, PCT International Publication No. WO 98/42393discloses a parenteral fluid transfer apparatus useful as a bloodcollection assembly, which includes an intravenous needle assemblyhaving a rod or probe-like blunting member which is extendable beyondthe tip of the intravenous needle tip to prevent accidental needle-stickwounds from occurring after use of the device. Such a device, however,does not provide protection for the second end of the needle at thenon-patient end of the assembly.

Accordingly, a need exists for a blood collection set with a non-patientneedle assembly which provides for safety blunting of the non-patientneedle tip and which is simple to manufacture and easy to operate.

SUMMARY OF THE INVENTION

The present invention is directed to a non-patient safety needleassembly for mounting with a conventional intravenous blood collectionset including a non-patient hub assembly having opposing first andsecond ends and a central opening extending through the hub assemblyfrom the first end to the second end. The first end being adapted formounting with a blood collection set. The needle assembly also includesan internal blunting member in fixed engagement with the non-patient hubassembly and extending through the central opening of the hub assembly,with the internal blunting member having a first end concentric with thenon-patient hub assembly. The needle assembly also includes a second endof the blunting member having a blunted tip and an internal lumenextending through the internal blunting member from the first end of theblunting member to the blunted tip. The needle assembly further includesan external non-patient cannula concentric with the internal bluntingmember and axially displaceable within the non-patient hub assembly,with the external non-patient cannula including a non-patient puncturetip adjacent the blunted tip of the internal blunting member. The needleassembly further includes an external non-patient cannula adapted foraxial displacement with respect to the non-patient hub assembly aboutthe internal blunting member between a first retracted position in whichthe non-patient puncture tip extends beyond the blunted tip of theinternal blunting member and a second activated position in which theblunted tip of the internal blunting member extends beyond thenon-patient puncture tip of the external non-patient cannula. The needleassembly further includes a sleeve extending about the non-patientpuncture tip, wherein the non-patient puncture tip can be inserted intoand removed from a blood collection tube having a pierceable membranewhile the external non-patient cannula is in the first retractedposition.

The non-patient safety needle assembly may further include a carriageassembly integral with the external non-patient cannula and concentricwith the internal blunting member, with the carriage assembly providedfor slidable engagement with the non-patient hub assembly.

The non-patient safety needle assembly may further include a fitting forengagement with a blood collection set. The fitting may include a luerfitting.

The non-patient safety needle assembly may further include means forattaching the non-patient needle assembly to a holder capable of holdingblood collection tubes. The attaching means may include threadsextending circumferentially about the non-patient hub assembly.

The non-patient safety needle assembly may be configured such that theexternal non-patient cannula is axially displaceable between the firstretracted position and the second activated position in a single axialdirection. The non-patient safety needle assembly may further include alocking mechanism for preventing axial displacement of the externalcannula from the second activated position to the first retractedposition.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a perspective view of a blood collection set in accordancewith the present invention, including a non-patient safety needleassembly attached to an intravenous needle assembly through tubing.

FIG. 2 is a perspective view of a non-patient safety needle assembly inaccordance with the present invention shown in a retracted position.

FIG. 3 is a side cross-sectional view of the non-patient safety needleassembly of FIG. 2 shown in a retracted position.

FIG. 4 is a perspective view of the non-patient safety needle assemblyof FIG. 2 shown in an activated blunted position.

FIG. 5 is a side cross-sectional view of the non-patient safety needleassembly of FIG. 4 in an activated blunted position.

DETAILED DESCRIPTION

While the present invention is satisfied by embodiments in manydifferent forms, there is shown in the drawings and will herein bedescribed in detail, the preferred embodiments of the invention, withthe understanding that the present disclosure is to be considered asexamplary of the principles of the invention and is not intended tolimit the invention to the embodiments illustrated. Various otherembodiments will be apparent to and readily made by those skilled in theart without departing from the scope and spirit of the invention. Thescope of the invention will be measured by the appended claims and theirequivalents.

Referring to the drawings in which like reference characters refer tolike parts throughout the several views thereof, FIG. 1 illustrates ablood collection set in accordance with the present invention and therelated features. The present invention is generally described in termsof a blood collection set, and encompasses such a blood collection setas well as a non-patient safety needle assembly for use in such a bloodcollection set.

Blood collection set 10 is depicted generally including non-patientneedle assembly 12 in engagement with a conventional intravenous bloodcollection assembly. Non-patient needle assembly 12 and the intravenousblood collection assembly include interrelating elements to provide forengagement therebetween. In particular, non-patient needle assembly 12is interconnected with intravenous needle assembly 90 through tubing 84.Such interconnection may be provided through any method as is known inthe art, such as through a luer fitting.

Intravenous needle assembly 90 includes an intravenous cannula 92 havingan intravenous puncture tip 94, for insertion into the vein of apatient, for example, during a blood collection procedure. Intravenousneedle assembly 90 further includes a butterfly-type wing assembly 96for use in connection with positioning and placement of intravenousneedle assembly 90 during a blood collection procedure, as is known inthe art.

As noted, intravenous needle assembly 90 is interconnected throughtubing 84 to non-patient needle assembly 12. In addition, non-patientneedle assembly 12 may be provided with means for attachment to aseparate holder (not shown) for use in connection with blood collectiontubes, such as a snap fit attachment, or, more desirably, attachmentthreads 14 which engage a threaded section of the holder.

Non-patient needle assembly 12 of the present invention is shown moreparticularly at FIGS. 2-5. Non-patient needle assembly 12 includes hubassembly 20 having first end 22 and second end 24, with an internalopening 26 extending therethrough from first end 22 to second end 24.First end 22 of hub assembly 20 is adapted for mounting with tubing 84of blood collection set 10. For example, hub assembly 20 may furtherinclude ferrule 30 extending from first end 22. Ferrule 30 may beintegrally formed with hub assembly 20, or may be a separate memberattached to hub assembly 20. Desirably, hub assembly 20 includesshoulder 34 at an internal opening within first end 22 for engagementwith ferrule 30 such that ferrule 30 interfits within first end 22 andrests against shoulder 34 of hub assembly 20. Ferrule 30 includes aninternal opening 36 extending therethrough, which is in fluidcommunication with internal opening 26 of hub assembly 20.

Non-patient needle assembly 12 further includes internal blunting member40 in fixed engagement with hub assembly 20. Internal blunting member 40is a generally tubular hollow structure which includes first end 42 andsecond end 44 with a central bore or internal lumen 48 extending throughthe length thereof. Internal lumen 48 allows fluid flow through needleassembly 12 during use. Second end 44 is blunted to form blunt tip 46 asan end portion, such that, under ordinary hand pressure, blunt tip 46will not easily puncture human skin or other biological tissue.

Internal blunting member 40 is provided in concentric relation with hubassembly 20. More particularly, first end 42 of internal blunting member40 is positioned concentrically within internal opening 26 of hubassembly 20, while second end 44 of internal blunting member 40 extendsaxially from second end 22 of hub assembly 20. Internal lumen 48 is influid communication with internal opening 26 of hub assembly 20 and, inturn, internal opening 36 of ferrule 30. Internal blunting member 40 maybe integrally formed with hub assembly 20, but is more desirably aseparate member which is fixedly attached to hub assembly 20. Inparticular, as depicted in FIG. 3, first end 42 of internal bluntingmember 40 is provided within internal opening 26 of hub assembly 20 andabuts lip 38 of ferrule 30, which extends within first end 22 of hubassembly 20. In this manner, hub assembly 20, ferrule 30, and internalblunting member 40 form a single unitary structure.

Non-patient needle assembly 12 further includes external cannula 50extending concentrically about internal blunting member 40. Externalcannula 50 is adapted for axial movement with respect to hub assembly20, as will be described in more detail herein. External cannula 50includes a first end 52 and a second end 54, with a central bore orinternal lumen 58 extending through the length thereof. Second end 54includes non-patient puncture tip 56, which is provided in the form of aneedle tip for puncturing a stopper such as is used in an evacuatedtube, for example, during a blood collection procedure. External cannula50 is further provided with an elastomeric sleeve 80 extending aboutsecond end 44 and covering non-patient puncture tip 56, as is generallyknown in the art.

As best depicted in FIGS. 2 and 3, second end 54 of external cannula 50is adjacent second end 44 of internal blunting member 40. Externalcannula 50 is axially slidable along second end 44 of internal bluntingmember 40 within the internal lumen 58 of external cannula 50. As such,external cannula 50 is axially displaceable with respect to hub assembly20, since internal blunting member 40 is in fixed engagement with hubassembly 20. The inner diameter of external cannula 50 is substantiallythe same as the outer diameter of second end 44 of internal bluntingmember 40. As such, external cannula 50 and internal blunting member 40are dimensioned and configured for a close fit so that blunt tip 46 ofinternal blunting member 40 lies flat against the internal surface ofsecond end 54 of external cannula 50 within internal lumen 58 whennon-patient needle assembly 12 is in a retracted position, as shown inFIGS. 2 and 3, and so that non-patient puncture tip 56 lies flat againstthe external surface of second end 44 of internal blunting member 40when non-patient needle assembly 12 is in an activated position, asshown in FIGS. 4 and 5.

It may be desirable to lubricate the mating surfaces of external cannula50 and internal blunting member 40, as well as to provide a seal betweenthem to prevent the unwanted flow of air bubbles. Accordingly, a drop ofviscous sealant-lubricant, such as petroleum jelly, may be providedabout the mating surfaces thereof.

As noted, external cannula 50 is adapted for axial movement with respectto hub assembly 20. For example, external cannula 50 may be axiallyslidable within internal opening 26 of hub assembly 20 between a firstretracted position in which non-patient puncture tip 56 extends beyondblunt tip 46, and a second activated position in which blunt tip 46extends beyond non-patient puncture tip 56. More particularly, axialmovement of external cannula 50 within internal opening 26 of hubassembly 20 in a direction of arrow 100 causes external cannula 50 toaxially displace with respect to hub assembly 20. Since internalblunting member 40 is fixedly attached to hub assembly 20, such axialdisplacement causes external cannula 50 to axially slide along secondend 44 of internal blunting member 40. Since second end 54 of externalcannula 50 is adjacent second end 44 of internal blunting member 40 andnon-patient puncture tip 56 extends beyond blunt tip 46, such axialmovement causes second end 54 of external cannula 50 to axially displacewith respect to second end 44 of internal blunting member 40, whichcauses non-patient puncture tip 56 to slide about internal bluntingmember 40 such that blunt tip 46 extends beyond non-patient puncture tip56, as depicted in FIGS. 4 and 5. As such, non-patient puncture tip 56is blunted.

Slidable engagement of external cannula 50 and hub assembly 20 may beeffected through carriage assembly 60. Carriage assembly 60 isconcentric with external cannula 50, and is provided for slidableengagement within internal opening 26 of hub assembly 20. Carriageassembly 60 may be integral with external cannula 50, or may be aseparate member which is fixedly adhered to external cannula 50 such asthrough the use of an adhesive. Carriage assembly 60 is defined by agenerally tubular body, although other shapes or configurations may beapparent to those skilled in the art.

Carriage assembly 60 includes a central nub portion 62, a forwardportion 64 and a rear portion 66. As shown in FIGS. 2 and 3, forwardportion 64 of carriage assembly 60 is positioned within internal opening26 of hub assembly 20 when non-patient needle assembly 12 is assembledand in the retracted position. Forward portion 64 of carriage assembly60 includes a surface 70 for interference engagement with shoulder 28 ofhub assembly 20. Such interference engagement prevents carriage assembly60, and therefore external cannula 50 which is attached thereto, frombeing easily removed or disassembled from hub assembly 20 after assemblythereof.

Central nub portion 62 includes a tapered surface 68 extendingcircumferentially thereabout. Tapered surface 68 provides aninterference engagement with face 32 at second end 24 of hub assembly20, preventing axial displacement of carriage assembly 60 with respectto hub assembly 20 without a force exerted thereon, as will be describedin more detail herein.

Carriage assembly 60 further includes rear face 72 which is adapted forengagement with the top surface of a blood collection tube during use.As will be discussed with respect to the use and operation ofnon-patient needle assembly 12, rear face 72 provides a mechanism foractivating non-patient needle assembly 12, thereby axially displacingexternal cannula 50 with respect to hub assembly 20 between a firstretracted position and a second activated position.

External cannula 50 and hub assembly 20 may be reversibly axiallydisplaceable with respect to each other, such that external cannula 50may displace with respect to hub assembly 20 from either the firstretracted position to the second activated position or from the secondactivated position to the first retracted position. In preferredembodiments, external cannula 50 is axially displaceable with respect tohub assembly 20 in only a single direction from the first retractedposition to the second activated position. As such, non-patient needleassembly 12 may be provided with means for preventing axial displacementof external cannula 50 from the second activated position to the firstretracted position once it has been activated, such as a lockingmechanism. For example, central nub portion 62 may further include asurface 76 which extends circumferentially about central nub portion 62for interference engagement with shoulder 28 of hub assembly 20 afteractivation of non-patient needle assembly 12 from the first retractedposition to the second activated position. Such interference engagementprevents axial movement of carriage assembly 60 with respect to hubassembly 20 in a direction opposite arrow 100 after movement from thefirst retracted position to the second activated position.

Non-patient needle assembly 12 may be provided with means for indicatingmovement of external cannula 50 with respect to hub assembly 20 betweenthe first retracted position and the second activated position. Suchmeans may be a visible, audible, and/or tactile indicator identifyingmovement between the first retracted position and the second extendedposition. For example, in one particular embodiment, a tactileindication is accomplished through the interference engagement oftapered surface 68 with face 32 of hub assembly 20, as well as theinterference engagement of front face 74 of carriage assembly 60 withface 32 of hub assembly 20. For example, when carriage assembly 60 isaxially displaced in a direction of arrow 100, the user will detect anaudible and/or tactile detection through the forcing of tapered surface68 of carriage assembly 60 past face 32 of hub assembly 20. Whencarriage assembly 60 is completely displaced to the second activatedposition, a further audible and/or tactile detection will be detected byfront face 74 of carriage assembly 60 abutting with face 32 of hubassembly 20.

Non-patient needle assembly 12 may be provided with a needle cover (notshown) for covering non-patient puncture tip 56 of external cannula 50prior to assembling of non-patient needle assembly 12 with a needleholder. Such a needle cover may be constructed of rigid polymericmaterial. This needle cover may be attached to non-patient needle holder12, for example, by threaded engagement with external threads 14extending about hub assembly 20. In this manner, this needle cover canbe removed from non-patient needle assembly 12 prior to assembly with aneedle holder by unthreading the needle cover from external threads 14,and then threading external threads 14 into an internal thread of such aneedle holder, as is known in the art.

Operation and use of the blood collection set including the non-patientneedle assembly will now be described with reference to FIGS. 1-5. Inuse, blood collection set 10 is provided including intravenous needleassembly 90 and non-patient needle assembly 12 attached through tubing84. Alternatively, non-patient needle assembly 12 may be provided asseparate from a blood collection assembly including intravenous needleassembly 90 and tubing 84 interconnected. In such a case, non-patientneedle assembly 12 is first attached to tubing 84, for example, throughconnector 86 which is desirably a luer fitting for connection withferrule 30.

Non-patient needle assembly 12 is provided including a needle cover (notshown) extending over external cannula 50. When preparing the bloodcollection set for use in a sampling procedure, the needle cover isremoved from external cannula 50, and non-patient needle assembly 12 isthen attached to a needle holder, such as by threading external threads14 with internal threads provided on a standard needle holder.

Moreover, a further needle cover (not shown) may extend over intravenouscannula 92 encompassing intravenous puncture tip 94. This needle coveris also removed. Venipuncture is then conducted in known manner, wherebyintravenous puncture tip 94 is inserted into a vein of a patient, and anevacuated tube having a pierceable closure is inserted into the needleholder, such that the pierceable closure of the evacuated tube contactssleeve 80 extending about external cannula 50. When slight pressure isexerted on the evacuated tube, the pierceable closure contacting sleeve80 causes sleeve 80 to displace, thereby causing non-patient puncturetip 56 to puncture sleeve 80 and, in turn, the pierceable closure of theevacuated tube. At such time, the interior of the evacuated tube andinternal lumen 58 of external cannula 50 are in fluid communication.Since the interior of the evacuated tube is at a negative pressure,blood is drawn from the vein of the patient, through intravenous needleassembly 90, through tubing 84 and connector 86, through internalopening 36 of ferrule 30, through internal lumen 48 of internal bluntingmember 40, through internal lumen 58 of external cannula 50, and intothe evacuated tube.

When all desired samples have been drawn, activation of the non-patientneedle assembly is accomplished. Activation of the non-patient needleassembly is desirably accomplished while venipuncture is maintained,that is while intravenous puncture tip 94 of intravenous needle assembly90 is maintained within the vein of the patient. It is noted thatintravenous needle assembly 90 may include a blunting member forblunting of the intravenous needle, which blunting operation is separatefrom blunting of the non-patient needle.

Blunting of the non-patient needle assembly 12 is accomplished byexerting pressure in a direction of arrow 100 on rear face 72 ofcarriage assembly 60. In particular, during sampling, the top surface ofthe pierceable closure of the evacuated tube contacts rear face 72 ofcarriage assembly 60 within the holder. When additional force is exertedagainst the evacuated tube in a direction of arrow 100, rear face 72 isforced in the direction of arrow 100. Such force causes interferenceengagement between tapered surface 68 of central nub portion 62 ofcarriage assembly 60 against face 32 of hub assembly 20. As such,central nub portion 62 of carriage 60 is forced within internal opening26 of hub assembly 20 due to the configuration of tapered surface 82,thereby causing axial movement of carriage assembly 60 with respect tohub assembly 20.

Since carriage assembly 60 is attached to external cannula 50, axialdisplacement of carriage assembly 60 with respect to hub assembly 20causes axial displacement of external cannula 50 with respect to hubassembly 20. Moreover, since internal blunting member 40 is attached tohub assembly 20, axial displacement of external cannula 50 with respectto hub assembly 20 causes second end 54 of external cannula 50 toaxially displace with respect to second end 44 of internal bluntingmember 40. Since blunted tip 44 is positioned short of non-patientpuncture tip 56 such that non-patient puncture tip 56 extends beyondblunted tip 44, axial displacement of second end 54 of external cannula50 with respect to second end 44 of internal blunting member 40 causesrelative axial displacement of non-patient puncture tip 56 with respectto blunted tip 46. More particularly, when external cannula 50 isaxially displaced in the direction of arrow 100, non-patient puncturetip 56 slides about internal blunting member 40 such that blunted tip 46is exposed and extends beyond non-patient puncture tip 56, as depictedin FIGS. 4 and 5. As such, non-patient puncture tip 56 is effectivelyblunted. Non-patient needle assembly 12 can then be appropriatelydiscarded.

As noted, the needle assembly of the present invention may be used inconjunction with a standard needle holder known for use in bloodcollection. It is also contemplated that the needle assembly of thepresent invention may be used with a needle holder which includes amechanism for causing axial displacement of carriage assembly 60 withrespect to hub assembly 20 to effect blunting of non-patient puncturetip 56. For example, as opposed to exerting pressure on an evacuatedtube extending within the needle holder, a mechanism on or within theneedle holder may be activated which causes carriage assembly 60 toaxially displace.

The needle assembly of the present invention may be comprised ofmoldable parts which can be mass produced from a variety of materialsincluding, for example, polyethylene, polyvinyl chloride, polystyrene orthe like. Materials will be selected which will provide the propersupport for the structure of the invention in its use, but which willalso provide a degree of resiliency for the purpose or providing thecooperative relative movement.

While the needle assembly of the present invention has been described interms of one embodiment for use in connection with a blood collectionsystem, it is further contemplated that the needle assembly could beused with other medical procedures, such as in conjunction with aconventional intravenous infusion set, as which are well known in theart for use with conventional needle assemblies.

1. A non-patient safety needle assembly for mounting with a conventionalintravenous blood collection set comprising: a non-patient hub assemblyhaving opposing first and second ends and a central opening extendingthrough said hub assembly from said first end to said second end, saidfirst end adapted for mounting with a blood collection set, an internalblunting member in fixed engagement with said non-patient hub assemblyand extending through said central opening of said hub assembly, saidinternal blunting member having a first end concentric with saidnon-patient hub assembly, a second end of said blunting member having ablunted tip and an internal lumen extending through said internalblunting member from said first end of said blunting member to saidblunted tip, an external non-patient cannula concentric with saidinternal blunting member and axially displaceable within saidnon-patient hub assembly, said external non-patient cannula including anon-patient puncture tip adjacent said blunted tip of said internalblunting member, said external non-patient cannula adapted for axialdisplacement with respect to said non-patient hub assembly about saidinternal blunting member between a first retracted position in whichsaid non-patient puncture tip extends beyond said blunted tip of saidinternal blunting member and a second activated position in which saidblunted tip of said internal blunting member extends beyond saidnon-patient puncture tip of said external non-patient cannula, and asleeve extending about said non-patient puncture tip, wherein saidnon-patient puncture tip can be inserted into and removed from a bloodcollection tube having a pierceable membrane while said externalnon-patient cannula is in said first retracted position.
 2. Anon-patient safety needle assembly as in claim 1, further comprising acarriage assembly integral with said external non-patient cannula andconcentric with said internal blunting member, said carriage assemblyprovided for slidable engagement with said non-patient hub assembly. 3.A non-patient safety needle assembly as in claim 1, further comprising afitting for engagement with a blood collection set.
 4. A non-patientsafety needle assembly as in claim 3, wherein said fitting comprises aluer fitting.
 5. A non-patient safety needle assembly as in claim 1,further comprising means for attaching said non-patient needle assemblyto a holder capable of holding blood collection tubes.
 6. A non-patientsafety needle assembly as in claim 5, wherein said attaching meanscomprises threads extending circumferentially about said non-patient hubassembly.
 7. A non-patient safety needle assembly as in claim 1, whereinsaid external non-patient cannula is axially displaceable between saidfirst retracted position and said second activated position in a singleaxial direction.
 8. A non-patient safety needle assembly as in claim 7,further comprising a locking mechanism for preventing axial displacementof said external cannula from said second activated position to saidfirst retracted position.